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Muscle Hypotonia clinical trials

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NCT ID: NCT03031808 Recruiting - Clinical trials for Intubation Complication

Comparison of Two Induction Regimens Using Topical Lidocaine or Muscle Relaxant on Sore Throat and Hemodynamics

Start date: October 31, 2017
Phase: Phase 4
Study type: Interventional

When a surgical procedure is performed under general anesthesia, the Airways are often secured With an endotracheal tube. Some patients experience sore throat thereafter. Studies have shown a reduction of these side effects when by use of muscle relaxants or a lidocain spray prior to the intubation. At Ostfold Hospital Trust, the investigators use one of the two methods or nothing. These methods will be studied systematically. Heart rate and blood pressure rise during the intubation procedure. The investigators will also study the differences between the groups.

NCT ID: NCT02696837 Completed - Inguinal Hernia Clinical Trials

Pediatric Inguinal Hernia Repair: Are Muscle Relaxants Necessary? Endotracheal Intubation vs Laryngeal Mask Airway

Start date: March 2016
Phase: N/A
Study type: Interventional

In prospective, safety-control study; children undergoing laparoscopic inguinal hernia repair using PIRS (Percutaneous Internal Ring Suturing) method will be randomly assigned into four groups. Gr 1: Endotracheal intubation and muscle relaxant, Gr 2: Endotracheal Intubation without muscle relaxant, Gr 3: Proseal Laryngeal Mask Airway without muscle relaxant, Gr 4: Proseal Laryngeal Mask Airway with subparalytic does muscle relaxant. Apart from standard monitorization, all patients' intragastric pressures will also be monitored. Patients' age at presentation, gender, time of surgery, time of anesthesia, intragastric pressure, intraabdominal pressure, intraoperative findings and complications will be noted and compared between groups.

NCT ID: NCT02685319 Completed - Flaccid Muscle Tone Clinical Trials

Mapping Human Muscle Satellite Cell Fate By Real-Time Imaging

S48
Start date: February 2016
Phase: N/A
Study type: Interventional

Mapping Human Muscle Satellite Cell Fate By Real-Time Imaging

NCT ID: NCT02640443 Enrolling by invitation - Clinical trials for Isolated PREPL Deficiency

Sulfamethoxazole for the Treatment of Primary PREPL Deficiency

SPPD
Start date: October 2015
Phase: Phase 2
Study type: Interventional

The investigators will evaluate whether sulfamethoxazole, a sulfamide antibiotic, improves the symptoms of primary PREPL deficiency (hypotonia-cystinuria syndrome and isolated PREPL deficiency).

NCT ID: NCT02575716 Completed - Muscle Relaxant Clinical Trials

Comparison of Intubating Condition of the Mcgrath Videolaryngoscope With and Without Muscle Relaxant

Start date: March 2013
Phase: Phase 1
Study type: Interventional

The objective of this study was to evaluate intubating condition using the McGrath® VL Series 5, with and without muscle relaxant

NCT ID: NCT02467595 Enrolling by invitation - Muscle Relaxants Clinical Trials

The Effect of no Muscle Relaxant Versus Reduced-dose Rocuronium on Anesthesia in Adenotonsillectomy

Start date: July 2015
Phase: Phase 4
Study type: Interventional

This study aimed to compare the effect of no muscle relaxants and reduced-dose rocuronium on the anesthetic induction and emergence with fentanyl in children undergoing adenotonsillectomy.

NCT ID: NCT02449369 Completed - Clinical trials for Unilateral Knee Arthroplasty

Intra-Venous Acetaminophen and Muscle Relaxants After Total Knee

IVAM
Start date: April 2015
Phase: Phase 4
Study type: Interventional

This is a prospective, three-arm, randomized, open-label trial to determine if a new pain control protocol which includes regular dosing of intravenous acetaminophen and orphenadrine for 48 hours after total knee surgery reduces the need for opioid pain medication and reduces average pain scores.

NCT ID: NCT02442128 Completed - Clinical trials for Anesthesia Intubation Complication

Fentanyl and Propofol for Tracheal Intubation During Sevoflurane Induction Without Muscle Relaxants in Children

Start date: June 2015
Phase: N/A
Study type: Interventional

Several methods have been proposed to improve intubating conditions and minimize sevoflurane induction time during sevoflurane induction in children. These include clonidine premedication, [5] addition of nitrous oxide, [6] opioids, [7,8] or propofol [9]. Four Studies evaluated sevoflurane alone for intubation (9-12).Aim of this study: is to evaluate the effects of two different dose of propofol preceded by a fixed dose of fentanyl during sevoflurane induction on quality of tracheal intubation in children undergoing elective surgery.

NCT ID: NCT02425449 Completed - Muscle Relaxants Clinical Trials

Fade Upon TOF Stimulation Induced by Succinylcholine

Start date: April 2015
Phase: Phase 4
Study type: Interventional

Muscle relaxants are medications used during surgery to facilitate surgical access. The effect of the muscle relaxant medications is measured by stimulation a motor nerve and measuring the force of the resultant muscle contraction. Based on the mechanism of action, two kinds of muscle relaxants are described. First a nondepolarizing muscle relaxant and the second kind is the depolarizing muscle relaxant. These two kinds of muscle relaxants can be distinguished by rapidly stimulating the nerve 4 times over 2 seconds (Train of four or TOF). The nondepolarizing muscle relaxants produce fade ie successive muscle contractions are less forceful than the preceding ones. Whereas the depolarizing muscle relaxants are generally believed to produce four contractions of equal strength. However, there is some indication that this may not be entirely correct. There is evidence that depolarizing muscle relaxants also may produce fade. The investigators are conducting the following study to determine if indeed depolarizing muscle relaxants produce fade. The investigators would also like to characterize the fade ie differences during onset and offset of the block and the effect of the dose on the degree on the fade.

NCT ID: NCT02263781 Not yet recruiting - Obesity Clinical Trials

PREPL in Health and Disease

PHD
Start date: October 2014
Phase: N/A
Study type: Interventional

Evaluation of PREPL activity in healthy controls and known or possible PREPL deficient patients